Twenty-four hour antihypertensive efficacy of indapamide, 1.5-mg sustained release: Results of two randomized double-blind controlled studies

被引:29
作者
Mallion, JH
Asmar, R
Boutelant, S
Guez, D
机构
[1] Inst Rech Int Servier, F-92415 Courbevoie, France
[2] Hop Broussais, Serv Med Interne 1, F-75674 Paris, France
[3] CHU Grenoble, Serv Med Interne & Cardiol, F-38043 Grenoble, France
关键词
hypertension; diuretic; indapamide; blood pressure monitoring; trough-to-peak ratio;
D O I
10.1097/00005344-199810000-00023
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The antihypertensive efficacy of a 1.5-mg sustained-release formulation (SR 1.5) of indapamide, a diuretic related to thiazide, has been pointed out by using conventional sphygmomanometric measurement 24 h after dosing in clinic, in two large European randomized, double-blind, controlled studies (2 and 3 months). One of these studies was then extended to 12 months, as a complementary open study. Quality controlled ambulatory blood pressure monitoring (ABPM) data for a total of 216 patients from these studies are presented, including subgroups of hypertensives and responders. Indapamide SR 1.5 achieves an adequate 24-h blood pressure control by significantly reducing the 24-h, diurnal, and nocturnal blood pressures versus baseline, confirming the sphygmomanometric data. The benefit at 2 and 3 months is maintained at 1 year, which confirms the long-term efficacy of SR 1.5 mg. The trough-to-peak ratio-not previously calculated for a diuretic according to international guidelines-meets Food and Drug Administration requirements and confirms the 24-h efficacy of indapamide SR 1.5.
引用
收藏
页码:673 / 678
页数:6
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